IL197964A - A process for the production of bromobenzens is produced - Google Patents

A process for the production of bromobenzens is produced

Info

Publication number: IL197964A
Authority: IL; Israel
Prior art keywords: formula; process according; copper; bromo; compound
Prior art date: 2006-10-25

Application number

IL197964A

Other languages

English (en)

Hebrew (he)

Other versions

IL197964A0 (en

Original Assignee

Syngenta Ltd

Syngenta Participations Ag

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2006-10-25

Filing date

2009-04-05

Publication date

2013-11-28

2009-04-05 Application filed by Syngenta Ltd, Syngenta Participations Ag filed Critical Syngenta Ltd

2009-12-24 Publication of IL197964A0 publication Critical patent/IL197964A0/en

2013-11-28 Publication of IL197964A publication Critical patent/IL197964A/en

Links

238000000034 method Methods 0.000 title claims abstract description 52
238000004519 manufacturing process Methods 0.000 title claims abstract description 16
150000004768 bromobenzenes Chemical class 0.000 title description 3
RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims abstract description 27
239000010949 copper Substances 0.000 claims abstract description 27
229910052802 copper Inorganic materials 0.000 claims abstract description 25
150000001875 compounds Chemical class 0.000 claims abstract description 21
239000003054 catalyst Substances 0.000 claims abstract description 20
IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 claims abstract description 18
CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 claims abstract description 15
230000002378 acidificating effect Effects 0.000 claims abstract description 12
239000012736 aqueous medium Substances 0.000 claims abstract description 12
125000001309 chloro group Chemical group Cl* 0.000 claims abstract description 6
125000001246 bromo group Chemical group Br* 0.000 claims abstract description 5
238000005580 one pot reaction Methods 0.000 claims abstract description 5
125000001153 fluoro group Chemical group F* 0.000 claims abstract description 3
125000002346 iodo group Chemical group I* 0.000 claims abstract description 3
239000000203 mixture Substances 0.000 claims description 25
HVKCZUVMQPUWSX-UHFFFAOYSA-N 1-bromo-2,3-dichlorobenzene Chemical compound ClC1=CC=CC(Br)=C1Cl HVKCZUVMQPUWSX-UHFFFAOYSA-N 0.000 claims description 17
238000006243 chemical reaction Methods 0.000 claims description 11
LMBFAGIMSUYTBN-MPZNNTNKSA-N teixobactin Chemical compound C([C@H](C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H](CCC(N)=O)C(=O)N[C@H]([C@@H](C)CC)C(=O)N[C@@H]([C@@H](C)CC)C(=O)N[C@@H](CO)C(=O)N[C@H]1C(N[C@@H](C)C(=O)N[C@@H](C[C@@H]2NC(=N)NC2)C(=O)N[C@H](C(=O)O[C@H]1C)[C@@H](C)CC)=O)NC)C1=CC=CC=C1 LMBFAGIMSUYTBN-MPZNNTNKSA-N 0.000 claims description 8
239000007864 aqueous solution Substances 0.000 claims description 7
239000003960 organic solvent Substances 0.000 claims description 7
UHOVQNZJYSORNB-UHFFFAOYSA-N monobenzene Natural products C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 6
239000000417 fungicide Substances 0.000 claims description 5
UWOIDOQAQPUVOH-UHFFFAOYSA-N 2-bromo-1,3-dichlorobenzene Chemical compound ClC1=CC=CC(Cl)=C1Br UWOIDOQAQPUVOH-UHFFFAOYSA-N 0.000 claims description 4
239000003905 agrochemical Substances 0.000 claims description 4
230000000855 fungicidal effect Effects 0.000 claims description 3
238000005191 phase separation Methods 0.000 claims description 3
150000001555 benzenes Chemical class 0.000 claims description 2
230000000063 preceeding effect Effects 0.000 claims 3
229910052801 chlorine Inorganic materials 0.000 claims 1
239000000460 chlorine Substances 0.000 claims 1
125000001424 substituent group Chemical group 0.000 abstract description 3
239000007795 chemical reaction product Substances 0.000 description 12
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
239000011541 reaction mixture Substances 0.000 description 11
238000002360 preparation method Methods 0.000 description 10
JHJLBTNAGRQEKS-UHFFFAOYSA-M sodium bromide Chemical compound [Na+].[Br-] JHJLBTNAGRQEKS-UHFFFAOYSA-M 0.000 description 8
LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 8
238000007792 addition Methods 0.000 description 7
239000012954 diazonium Substances 0.000 description 7
150000001989 diazonium salts Chemical class 0.000 description 7
239000000543 intermediate Substances 0.000 description 7
229910021589 Copper(I) bromide Inorganic materials 0.000 description 6
NKNDPYCGAZPOFS-UHFFFAOYSA-M copper(i) bromide Chemical compound Br[Cu] NKNDPYCGAZPOFS-UHFFFAOYSA-M 0.000 description 6
239000007788 liquid Substances 0.000 description 6
BRPSAOUFIJSKOT-UHFFFAOYSA-N 2,3-dichloroaniline Chemical compound NC1=CC=CC(Cl)=C1Cl BRPSAOUFIJSKOT-UHFFFAOYSA-N 0.000 description 5
239000003513 alkali Substances 0.000 description 5
230000031709 bromination Effects 0.000 description 5
238000005893 bromination reaction Methods 0.000 description 5
239000012043 crude product Substances 0.000 description 5
238000011031 large-scale manufacturing process Methods 0.000 description 5
150000002826 nitrites Chemical class 0.000 description 5
239000012074 organic phase Substances 0.000 description 5
239000007787 solid Substances 0.000 description 5
239000000243 solution Substances 0.000 description 5
CPELXLSAUQHCOX-UHFFFAOYSA-N Hydrogen bromide Chemical compound Br CPELXLSAUQHCOX-UHFFFAOYSA-N 0.000 description 4
239000002253 acid Substances 0.000 description 4
239000008346 aqueous phase Substances 0.000 description 4
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 4
229910052794 bromium Inorganic materials 0.000 description 4
229910001503 inorganic bromide Inorganic materials 0.000 description 4
239000000047 product Substances 0.000 description 4
235000010288 sodium nitrite Nutrition 0.000 description 4
RLOHOBNEYHBZID-UHFFFAOYSA-N 3-(difluoromethyl)-1-methylpyrazole-4-carboxylic acid Chemical compound CN1C=C(C(O)=O)C(C(F)F)=N1 RLOHOBNEYHBZID-UHFFFAOYSA-N 0.000 description 3
BMYNFMYTOJXKLE-UHFFFAOYSA-N 3-azaniumyl-2-hydroxypropanoate Chemical compound NCC(O)C(O)=O BMYNFMYTOJXKLE-UHFFFAOYSA-N 0.000 description 3
BHELIUBJHYAEDK-OAIUPTLZSA-N Aspoxicillin Chemical compound C1([C@H](C(=O)N[C@@H]2C(N3[C@H](C(C)(C)S[C@@H]32)C(O)=O)=O)NC(=O)[C@H](N)CC(=O)NC)=CC=C(O)C=C1 BHELIUBJHYAEDK-OAIUPTLZSA-N 0.000 description 3
YMWUJEATGCHHMB-UHFFFAOYSA-N Dichloromethane Chemical compound ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 3
238000000297 Sandmeyer reaction Methods 0.000 description 3
YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
125000003118 aryl group Chemical group 0.000 description 3
230000015572 biosynthetic process Effects 0.000 description 3
150000001649 bromium compounds Chemical class 0.000 description 3
239000004009 herbicide Substances 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
-1 nitrite ester Chemical class 0.000 description 3
RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 2
PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 2
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 2
HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
125000001931 aliphatic group Chemical group 0.000 description 2
150000001450 anions Chemical class 0.000 description 2
239000012431 aqueous reaction media Substances 0.000 description 2
239000003795 chemical substances by application Substances 0.000 description 2
238000011065 in-situ storage Methods 0.000 description 2
238000002844 melting Methods 0.000 description 2
230000008018 melting Effects 0.000 description 2
IOLCXVTUBQKXJR-UHFFFAOYSA-M potassium bromide Chemical compound [K+].[Br-] IOLCXVTUBQKXJR-UHFFFAOYSA-M 0.000 description 2
239000000725 suspension Substances 0.000 description 2
238000005292 vacuum distillation Methods 0.000 description 2
239000002699 waste material Substances 0.000 description 2
LEFQPBAWVJEIJS-UHFFFAOYSA-N 1-bromo-2-chloro-4-fluorobenzene Chemical compound FC1=CC=C(Br)C(Cl)=C1 LEFQPBAWVJEIJS-UHFFFAOYSA-N 0.000 description 1
QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 1
AZFNGPAYDKGCRB-XCPIVNJJSA-M [(1s,2s)-2-amino-1,2-diphenylethyl]-(4-methylphenyl)sulfonylazanide;chlororuthenium(1+);1-methyl-4-propan-2-ylbenzene Chemical compound [Ru+]Cl.CC(C)C1=CC=C(C)C=C1.C1=CC(C)=CC=C1S(=O)(=O)[N-][C@@H](C=1C=CC=CC=1)[C@@H](N)C1=CC=CC=C1 AZFNGPAYDKGCRB-XCPIVNJJSA-M 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 1
230000009435 amidation Effects 0.000 description 1
238000007112 amidation reaction Methods 0.000 description 1
125000003277 amino group Chemical group 0.000 description 1
239000002635 aromatic organic solvent Substances 0.000 description 1
MXWJVTOOROXGIU-UHFFFAOYSA-N atrazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)C)=N1 MXWJVTOOROXGIU-UHFFFAOYSA-N 0.000 description 1
ILMCRZOMKCLIFZ-UHFFFAOYSA-N benzonorbornene Chemical compound C12=CC=CC=C2C2CCC1C2 ILMCRZOMKCLIFZ-UHFFFAOYSA-N 0.000 description 1
229910001622 calcium bromide Inorganic materials 0.000 description 1
WGEFECGEFUFIQW-UHFFFAOYSA-L calcium dibromide Chemical compound [Ca+2].[Br-].[Br-] WGEFECGEFUFIQW-UHFFFAOYSA-L 0.000 description 1
238000012512 characterization method Methods 0.000 description 1
150000001879 copper Chemical class 0.000 description 1
239000013078 crystal Substances 0.000 description 1
125000000664 diazo group Chemical group [N-]=[N+]=[*] 0.000 description 1
239000007789 gas Substances 0.000 description 1
230000020169 heat generation Effects 0.000 description 1
238000010438 heat treatment Methods 0.000 description 1
230000002363 herbicidal effect Effects 0.000 description 1
125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
239000012535 impurity Substances 0.000 description 1
OWFXIOWLTKNBAP-UHFFFAOYSA-N isoamyl nitrite Chemical compound CC(C)CCON=O OWFXIOWLTKNBAP-UHFFFAOYSA-N 0.000 description 1
238000002955 isolation Methods 0.000 description 1
OTCKOJUMXQWKQG-UHFFFAOYSA-L magnesium bromide Chemical compound [Mg+2].[Br-].[Br-] OTCKOJUMXQWKQG-UHFFFAOYSA-L 0.000 description 1
229910001623 magnesium bromide Inorganic materials 0.000 description 1
AAJBNRZDTJPMTJ-UHFFFAOYSA-L magnesium;dinitrite Chemical compound [Mg+2].[O-]N=O.[O-]N=O AAJBNRZDTJPMTJ-UHFFFAOYSA-L 0.000 description 1
239000002609 medium Substances 0.000 description 1
229940073584 methylene chloride Drugs 0.000 description 1
150000007522 mineralic acids Chemical class 0.000 description 1
DADSZOFTIIETSV-UHFFFAOYSA-N n,n-dichloroaniline Chemical compound ClN(Cl)C1=CC=CC=C1 DADSZOFTIIETSV-UHFFFAOYSA-N 0.000 description 1
150000007524 organic acids Chemical class 0.000 description 1
235000005985 organic acids Nutrition 0.000 description 1
239000002245 particle Substances 0.000 description 1
RAFRTSDUWORDLA-UHFFFAOYSA-N phenyl 3-chloropropanoate Chemical compound ClCCC(=O)OC1=CC=CC=C1 RAFRTSDUWORDLA-UHFFFAOYSA-N 0.000 description 1
235000010289 potassium nitrite Nutrition 0.000 description 1
239000004304 potassium nitrite Substances 0.000 description 1
239000000376 reactant Substances 0.000 description 1
239000012429 reaction media Substances 0.000 description 1
230000035484 reaction time Effects 0.000 description 1
238000011084 recovery Methods 0.000 description 1
239000012265 solid product Substances 0.000 description 1
239000002904 solvent Substances 0.000 description 1
239000007858 starting material Substances 0.000 description 1
239000001117 sulphuric acid Substances 0.000 description 1
235000011149 sulphuric acid Nutrition 0.000 description 1
IOGXOCVLYRDXLW-UHFFFAOYSA-N tert-butyl nitrite Chemical compound CC(C)(C)ON=O IOGXOCVLYRDXLW-UHFFFAOYSA-N 0.000 description 1
239000012414 tert-butyl nitrite Substances 0.000 description 1
238000010626 work up procedure Methods 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N29/00—Biocides, pest repellants or attractants, or plant growth regulators containing halogenated hydrocarbons
- A01N29/04—Halogen directly attached to a carbocyclic ring system
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C25/00—Compounds containing at least one halogen atom bound to a six-membered aromatic ring
- C07C25/02—Monocyclic aromatic halogenated hydrocarbons
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C17/00—Preparation of halogenated hydrocarbons
- C07C17/093—Preparation of halogenated hydrocarbons by replacement by halogens
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C25/00—Compounds containing at least one halogen atom bound to a six-membered aromatic ring
- C07C25/02—Monocyclic aromatic halogenated hydrocarbons
- C07C25/13—Monocyclic aromatic halogenated hydrocarbons containing fluorine

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Life Sciences & Earth Sciences (AREA)
Agronomy & Crop Science (AREA)
Pest Control & Pesticides (AREA)
Health & Medical Sciences (AREA)
Engineering & Computer Science (AREA)
Dentistry (AREA)
General Health & Medical Sciences (AREA)
Wood Science & Technology (AREA)
Zoology (AREA)
Environmental Sciences (AREA)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Steroid Compounds (AREA)

IL197964A 2006-10-25 2009-04-05 A process for the production of bromobenzens is produced IL197964A (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
EP06022279		2006-10-25
PCT/EP2007/008697 WO2008049507A1 (en)	2006-10-25	2007-10-08	Process for the production of substituted bromobenzenes

Publications (2)

Publication Number	Publication Date
IL197964A0 IL197964A0 (en)	2009-12-24
IL197964A true IL197964A (en)	2013-11-28

Family

ID=38722632

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
IL197964A IL197964A (en)	2006-10-25	2009-04-05	A process for the production of bromobenzens is produced

Country Status (18)

Country	Link
US (1)	US8088960B2 (de)
EP (1)	EP2076123B1 (de)
JP (1)	JP2010507600A (de)
KR (1)	KR20090075704A (de)
CN (1)	CN101528034B (de)
AT (1)	ATE511350T1 (de)
AU (1)	AU2007308423B2 (de)
BR (1)	BRPI0717985A2 (de)
CA (1)	CA2667499A1 (de)
DK (1)	DK2076123T3 (de)
ES (1)	ES2366561T3 (de)
IL (1)	IL197964A (de)
MX (1)	MX2009003979A (de)
PL (1)	PL2076123T3 (de)
RU (1)	RU2453524C2 (de)
TW (1)	TW200824566A (de)
UA (1)	UA95983C2 (de)
WO (1)	WO2008049507A1 (de)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JP5995445B2 (ja) *	2009-03-12	2016-09-21	バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングＢａｙｅｒＩｎｔｅｌｌｅｃｔｕａｌＰｒｏｐｅｒｔｙＧｍｂＨ	クロロ芳香族化合物及びブロモ芳香族化合物を調整する方法
MX2012012009A (es)	2010-04-20	2012-12-17	Syngenta Participations Ag	Proceso para preparar amidas de acidos carboxilicos pirazolicos.
CN102844306B (zh)	2010-04-20	2015-01-14	先正达参股股份有限公司	吡唑羧酸酰胺的制备方法
WO2011131545A1 (en)	2010-04-20	2011-10-27	Syngenta Participations Ag	Process for the preparation of pyrazole carboxylic acid amides
CN102001913B (zh) *	2010-11-23	2013-03-13	常州工程职业技术学院	一种2-氯-3-氟溴苯的合成方法
CN106748627A (zh) *	2016-11-14	2017-05-31	苏州市罗森助剂有限公司	一种一锅法制备3,5‑二甲基溴苯的方法
CN109134187B (zh) *	2018-06-26	2019-09-20	浙江中山化工集团股份有限公司	一种合成高立体阻碍的溴代苯的工艺
CN115872834B (zh) *	2021-09-29	2025-08-29	联化科技新材(台州)有限公司	一种3,4,5-三氟溴苯的制备方法
CN116082188A (zh) *	2023-02-14	2023-05-09	都创(上海)医药开发有限公司	一种以3-氟-4-氨基苯腈为原料合成4-溴-3-氯-5-氟苯腈的方法
CN116891399A (zh) *	2023-06-20	2023-10-17	清源创新实验室	一种2,5-二溴-1,3-二氯苯的制备方法

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPH075487B2 (ja)	1985-11-14	1995-01-25	住友化学工業株式会社	１―ブロモ―２―クロロ―４―フルオロベンゼンの製造法
JP2000256285A (ja) *	1999-03-15	2000-09-19	Nippon Chemiphar Co Ltd	２−（イソブチルメチルアミノ）ベンジルアルコールの製造方法

2007
- 2007-10-08 EP EP07818772A patent/EP2076123B1/de active Active
- 2007-10-08 KR KR1020097008493A patent/KR20090075704A/ko not_active Ceased
- 2007-10-08 MX MX2009003979A patent/MX2009003979A/es active IP Right Grant
- 2007-10-08 WO PCT/EP2007/008697 patent/WO2008049507A1/en not_active Ceased
- 2007-10-08 UA UAA200904497A patent/UA95983C2/ru unknown
- 2007-10-08 RU RU2009119353/04A patent/RU2453524C2/ru not_active IP Right Cessation
- 2007-10-08 JP JP2009533684A patent/JP2010507600A/ja active Pending
- 2007-10-08 AT AT07818772T patent/ATE511350T1/de active
- 2007-10-08 US US12/446,793 patent/US8088960B2/en not_active Expired - Fee Related
- 2007-10-08 CN CN2007800398500A patent/CN101528034B/zh active Active
- 2007-10-08 AU AU2007308423A patent/AU2007308423B2/en not_active Ceased
- 2007-10-08 DK DK07818772.1T patent/DK2076123T3/da active
- 2007-10-08 CA CA002667499A patent/CA2667499A1/en not_active Abandoned
- 2007-10-08 TW TW096137665A patent/TW200824566A/zh unknown
- 2007-10-08 PL PL07818772T patent/PL2076123T3/pl unknown
- 2007-10-08 ES ES07818772T patent/ES2366561T3/es active Active
- 2007-10-08 BR BRPI0717985-5A patent/BRPI0717985A2/pt not_active IP Right Cessation
2009
- 2009-04-05 IL IL197964A patent/IL197964A/en active IP Right Grant

Also Published As

Publication number	Publication date
CN101528034B (zh)	2011-11-09
WO2008049507A1 (en)	2008-05-02
TW200824566A (en)	2008-06-16
DK2076123T3 (da)	2011-08-29
ATE511350T1 (de)	2011-06-15
ES2366561T3 (es)	2011-10-21
JP2010507600A (ja)	2010-03-11
EP2076123B1 (de)	2011-06-01
BRPI0717985A2 (pt)	2013-11-12
CA2667499A1 (en)	2008-05-02
US8088960B2 (en)	2012-01-03
RU2453524C2 (ru)	2012-06-20
AU2007308423A1 (en)	2008-05-02
KR20090075704A (ko)	2009-07-08
IL197964A0 (en)	2009-12-24
MX2009003979A (es)	2009-04-27
RU2009119353A (ru)	2010-11-27
PL2076123T3 (pl)	2011-11-30
CN101528034A (zh)	2009-09-09
EP2076123A1 (de)	2009-07-08
UA95983C2 (ru)	2011-09-26
US20110065968A1 (en)	2011-03-17
AU2007308423B2 (en)	2011-10-06

Legal Events

Date	Code	Title
2014-03-31	FF	Patent granted
2014-03-31	KB	Patent renewed
2017-09-28	KB	Patent renewed
2021-10-31	KB	Patent renewed

Publication	Publication Date	Title
EP2076123B1 (de)	2011-06-01	Verfahren für die herstellung von substituierten brombenzolen
US5679879A (en)	1997-10-21	Process for the production of substituted aromatic hydrocarbons from corresponding anilines by dediazoniation
RU2359960C2 (ru)	2009-06-27	Способ производства 2,3-дихлорпиридина
AU770029B2 (en)	2004-02-12	Processes for preparing pesticidal intermediates
US4730046A (en)	1988-03-08	Preparation of aryl halides
HUP0700757A2 (en)	2010-04-28	Process for producing pharmaceutical intermediers
US2123857A (en)	1938-07-12	Manufacture of 1,3-dichloro-and 1, 3, 5-trichlorobenzenes
US4785121A (en)	1988-11-15	Preparation of halophthalic anhydrides
EP1334080A1 (de)	2003-08-13	1,3-bis(trifluormethyl)benzolderivate
EP0163230B2 (de)	1996-03-06	Verfahren zur Herstellung von chlorierten aromatischen Verbindungen
EP0014033B1 (de)	1983-02-16	Halogenierung von Pyridin-Verbindungen
Aroskar et al.	1964	572. Aromatic polyfluoro-compounds. Part XVIII. Some replacement reactions of perfluoro-o-and-p-xylene
US3304331A (en)	1967-02-14	Process for chlorination of dimethylsulfoxide
JPH0424341B2 (de)	1992-04-24
US5233104A (en)	1993-08-03	Process for trifluoromethylation of aromatic compounds
EP0037698A1 (de)	1981-10-14	Benzaldehydderivate zur Verwendung als chemisches Zwischenprodukt
CS212349B2 (en)	1982-03-26	Method of making the esters of the 3-/2-arylvinyl/-2,2- dimethyl-cyclopropan-1-carboxyl acids
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